Canonical Allele Identifier: PA2826096331
Gene: TMEM216 HGNC NCBI

Linked Data

ClinVar Variation Id: 1433371
ClinVar RCV Id: RCV001960088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167461.1:p.Phe75Cys
CA380685191
NM_001173990.3:c.224T>G